Conjugate-elimination on unsaturated acetals: A one-step route to functionalized 1,3-dienes.
- 1 November 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (47) , 8591-8594
- https://doi.org/10.1016/0040-4039(95)01832-3
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- A quantum mechanical study on carbocation formation energy in (poly)ethylenic compoundsTetrahedron Letters, 1994
- Conjugate Addition Reactions of Allylic Copper Species Derived from Grignard Reagents: Synthetic and Spectroscopic AspectsThe Journal of Organic Chemistry, 1994
- Evidence for a Cyclic Mechanism in (.eta.3-Allyl)palladium Chemistry. Promotion of .beta.-Hydride Elimination by Unsaturated OrganometallicsJournal of the American Chemical Society, 1994
- .alpha.,.beta.-Unsaturated Acetals as Precursors of .alpha.-Substituted Ethoxy Dienes. Useful Reagents for Nucleophilic AcylationThe Journal of Organic Chemistry, 1994
- 1-(Phenylthio)- and 1-(phenylsulfoxide)-4-alkoxy-butadienes, a new class of chiral dienes.Tetrahedron Letters, 1992
- A new prenylation method using the lithium enolate of prenal. Reaction with polyunsaturated aldehydes. A short access to retinal.Tetrahedron Letters, 1991
- Regio- and Stereocontrolled Stannylmetallation of 3,3-diethoxy-prop-1-yne and 4,4-diethoxy-but-1-yne : An efficient access to the corresponding vinyltins with fixed configurationsTetrahedron Letters, 1991
- Unexpected behavior of dienol thio ethers gives versatile access to a large set of functionalized dienesThe Journal of Organic Chemistry, 1991
- Crown thio ether chemistryAccounts of Chemical Research, 1988
- Reactivity of α,β-unsaturated acetals and ketals toward organolithium reagents in pentaneTetrahedron Letters, 1984